![18. M(0) carbonyl complexes with chelating di-NHC or tri-NHC ligands... | Download Scientific Diagram 18. M(0) carbonyl complexes with chelating di-NHC or tri-NHC ligands... | Download Scientific Diagram](https://www.researchgate.net/profile/Lu-Jiang-5/publication/272102102/figure/fig7/AS:572844640030720@1513588213462/M0-carbonyl-complexes-with-chelating-di-NHC-or-tri-NHC-ligands-72-73-115.png)
18. M(0) carbonyl complexes with chelating di-NHC or tri-NHC ligands... | Download Scientific Diagram
![Diastereoselective Carbonyl Allylation with Simple Olefins Enabled by Palladium Complex-Catalyzed C-H Oxidative Borylation Diastereoselective Carbonyl Allylation with Simple Olefins Enabled by Palladium Complex-Catalyzed C-H Oxidative Borylation](https://www.organic-chemistry.org/abstracts/lit4/880m.gif)
Diastereoselective Carbonyl Allylation with Simple Olefins Enabled by Palladium Complex-Catalyzed C-H Oxidative Borylation
![Iodide-enhanced palladium catalysis via formation of iodide-bridged binuclear palladium complex | Communications Chemistry Iodide-enhanced palladium catalysis via formation of iodide-bridged binuclear palladium complex | Communications Chemistry](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fs42004-020-0287-0/MediaObjects/42004_2020_287_Fig1_HTML.png)
Iodide-enhanced palladium catalysis via formation of iodide-bridged binuclear palladium complex | Communications Chemistry
![Bulky N‐Heterocyclic‐Carbene‐Coordinated Palladium Catalysts for 1,2‐Addition of Arylboron Compounds to Carbonyl Compounds - Okuda - 2020 - ChemCatChem - Wiley Online Library Bulky N‐Heterocyclic‐Carbene‐Coordinated Palladium Catalysts for 1,2‐Addition of Arylboron Compounds to Carbonyl Compounds - Okuda - 2020 - ChemCatChem - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/35b247d2-5c20-4191-bfe0-958bfdc6956d/cctc202001464-toc-0001-m.jpg)
Bulky N‐Heterocyclic‐Carbene‐Coordinated Palladium Catalysts for 1,2‐Addition of Arylboron Compounds to Carbonyl Compounds - Okuda - 2020 - ChemCatChem - Wiley Online Library
![Pyrazol-1-yl)carbonyl palladium complexes as catalysts for ethylene polymerization reaction - ScienceDirect Pyrazol-1-yl)carbonyl palladium complexes as catalysts for ethylene polymerization reaction - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0022328X12006250-fx1.jpg)
Pyrazol-1-yl)carbonyl palladium complexes as catalysts for ethylene polymerization reaction - ScienceDirect
![Palladium-catalysed carboformylation of alkynes using acid chlorides as a dual carbon monoxide and carbon source | Nature Chemistry Palladium-catalysed carboformylation of alkynes using acid chlorides as a dual carbon monoxide and carbon source | Nature Chemistry](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fs41557-020-00621-x/MediaObjects/41557_2020_621_Figa_HTML.png)
Palladium-catalysed carboformylation of alkynes using acid chlorides as a dual carbon monoxide and carbon source | Nature Chemistry
![Alternative Synthetic Methods for PEPPSI‐Type Palladium Complexes - Green - 2014 - European Journal of Inorganic Chemistry - Wiley Online Library Alternative Synthetic Methods for PEPPSI‐Type Palladium Complexes - Green - 2014 - European Journal of Inorganic Chemistry - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/b441183c-5410-4952-874f-59e6fedd6b64/mfig000.jpg)
Alternative Synthetic Methods for PEPPSI‐Type Palladium Complexes - Green - 2014 - European Journal of Inorganic Chemistry - Wiley Online Library
![Palladium‐Catalyzed Selective Reduction of Carbonyl Compounds - Sarkar - 2020 - European Journal of Inorganic Chemistry - Wiley Online Library Palladium‐Catalyzed Selective Reduction of Carbonyl Compounds - Sarkar - 2020 - European Journal of Inorganic Chemistry - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/0dd4ab0f-ae6a-4592-b1fe-79f1f4d6cceb/ejic202000310-fig-0001-m.jpg)
Palladium‐Catalyzed Selective Reduction of Carbonyl Compounds - Sarkar - 2020 - European Journal of Inorganic Chemistry - Wiley Online Library
![Asymmetric carbonyl-ene reaction of trifluoropyruvate catalyzed by Pd(II)-SunPhos complex - ScienceDirect Asymmetric carbonyl-ene reaction of trifluoropyruvate catalyzed by Pd(II)-SunPhos complex - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0040402017310724-fx1.jpg)
Asymmetric carbonyl-ene reaction of trifluoropyruvate catalyzed by Pd(II)-SunPhos complex - ScienceDirect
![Industrial catalyst | Palladium(+1) Carbonyl Clusters in the Catalytic Oxidation of Unsaturated Compounds Industrial catalyst | Palladium(+1) Carbonyl Clusters in the Catalytic Oxidation of Unsaturated Compounds](https://www.technology.matthey.com/wp-content/uploads/articles/47/1/pmr0047-0020-f1.gif)
Industrial catalyst | Palladium(+1) Carbonyl Clusters in the Catalytic Oxidation of Unsaturated Compounds
![Reduction of α,β-unsaturated carbonyl compounds by palladium(II) and nickel(II) complexes having nitrogen-containing ligands - ScienceDirect Reduction of α,β-unsaturated carbonyl compounds by palladium(II) and nickel(II) complexes having nitrogen-containing ligands - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S1381116908001969-fx1.jpg)
Reduction of α,β-unsaturated carbonyl compounds by palladium(II) and nickel(II) complexes having nitrogen-containing ligands - ScienceDirect
![Low Coordinate Germanium(II) and Tin(II) Hydride Complexes: Efficient Catalysts for the Hydroboration of Carbonyl Compounds | Chem-Station Int. Ed. Low Coordinate Germanium(II) and Tin(II) Hydride Complexes: Efficient Catalysts for the Hydroboration of Carbonyl Compounds | Chem-Station Int. Ed.](https://i2.wp.com/assets.en.chem-station.com/uploads/2014/03/ja-2014-006477_0005-1.gif?fit=500%2C204&ssl=1)
Low Coordinate Germanium(II) and Tin(II) Hydride Complexes: Efficient Catalysts for the Hydroboration of Carbonyl Compounds | Chem-Station Int. Ed.
![Unified and practical access to ɤ-alkynylated carbonyl derivatives via streamlined assembly at room temperature | Communications Chemistry Unified and practical access to ɤ-alkynylated carbonyl derivatives via streamlined assembly at room temperature | Communications Chemistry](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fs42004-019-0219-z/MediaObjects/42004_2019_219_Fig1_HTML.png)
Unified and practical access to ɤ-alkynylated carbonyl derivatives via streamlined assembly at room temperature | Communications Chemistry
![Palladium nanoparticles on amino-modified silica-catalyzed C–C bond formation with carbonyl insertion | SpringerLink Palladium nanoparticles on amino-modified silica-catalyzed C–C bond formation with carbonyl insertion | SpringerLink](https://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs13738-021-02171-6/MediaObjects/13738_2021_2171_Figa_HTML.png)
Palladium nanoparticles on amino-modified silica-catalyzed C–C bond formation with carbonyl insertion | SpringerLink
![One‐Pot Syntheses of α,β‐Unsaturated Carbonyl Compounds through Palladium‐Mediated Dehydrogenation of Ketones, Aldehydes, Esters, Lactones and Amides - Muzart - 2010 - European Journal of Organic Chemistry - Wiley Online Library One‐Pot Syntheses of α,β‐Unsaturated Carbonyl Compounds through Palladium‐Mediated Dehydrogenation of Ketones, Aldehydes, Esters, Lactones and Amides - Muzart - 2010 - European Journal of Organic Chemistry - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/389d7f1d-d09b-4821-a1e8-92d6da56276d/mformel1.jpg)
One‐Pot Syntheses of α,β‐Unsaturated Carbonyl Compounds through Palladium‐Mediated Dehydrogenation of Ketones, Aldehydes, Esters, Lactones and Amides - Muzart - 2010 - European Journal of Organic Chemistry - Wiley Online Library
![Proposed mechanism for the palladium pincer-catalyzed carbonylative... | Download Scientific Diagram Proposed mechanism for the palladium pincer-catalyzed carbonylative... | Download Scientific Diagram](https://www.researchgate.net/publication/330463065/figure/fig4/AS:716245808721921@1547777716698/Proposed-mechanism-for-the-palladium-pincer-catalyzed-carbonylative-Sonogashira-and.png)
Proposed mechanism for the palladium pincer-catalyzed carbonylative... | Download Scientific Diagram
Viable pathways for the oxidative addition of iodobenzene to palladium (0)-triphenylphosphine-carbonyl complexes: a theoretical study - Dalton Transactions (RSC Publishing)
![Binuclear Palladium Complex Immobilized on Mesoporous SBA-16: Efficient Heterogeneous Catalyst for the Carbonylative Suzuki Coupling Reaction of Aryl Iodides and Arylboronic Acids Using Cr(CO)6 as Carbonyl Source | SpringerLink Binuclear Palladium Complex Immobilized on Mesoporous SBA-16: Efficient Heterogeneous Catalyst for the Carbonylative Suzuki Coupling Reaction of Aryl Iodides and Arylboronic Acids Using Cr(CO)6 as Carbonyl Source | SpringerLink](https://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs10562-019-03087-w/MediaObjects/10562_2019_3087_Figa_HTML.png)
Binuclear Palladium Complex Immobilized on Mesoporous SBA-16: Efficient Heterogeneous Catalyst for the Carbonylative Suzuki Coupling Reaction of Aryl Iodides and Arylboronic Acids Using Cr(CO)6 as Carbonyl Source | SpringerLink
![Palladium-catalyzed allene synthesis enabled by β-hydrogen elimination from sp2-carbon | Nature Communications Palladium-catalyzed allene synthesis enabled by β-hydrogen elimination from sp2-carbon | Nature Communications](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fs41467-020-20740-w/MediaObjects/41467_2020_20740_Fig1_HTML.png)
Palladium-catalyzed allene synthesis enabled by β-hydrogen elimination from sp2-carbon | Nature Communications
![IUCr) Crystal structure of the new palladium complexes tetrakis(1,3-dimethylimidazolium-2-ylidene)palladium(II) hexadecacarbonyltetrarhenium diethyl ether disolvate and octa-μ-carbonyl-dicarbonyltetrakis(triphenylphosphane)palladiumdirhenium (unknown ... IUCr) Crystal structure of the new palladium complexes tetrakis(1,3-dimethylimidazolium-2-ylidene)palladium(II) hexadecacarbonyltetrarhenium diethyl ether disolvate and octa-μ-carbonyl-dicarbonyltetrakis(triphenylphosphane)palladiumdirhenium (unknown ...](https://journals.iucr.org/e/issues/2021/10/00/tx2041/tx2041scheme1.gif)